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Mdr jobs

91 jobs

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Programme Manager - MDR

ConvaTec

 ...better ways of delivering for our customers and each other. We're aiming for nothing short of excellence. Join us as Programme Manager - MDR and you'll do the same. About the role: As our Programme Manager, you'll be the driving force behind our critical MDR Project and will... 
Deeside, Flintshire
a month ago

MDR Consultant - North Yorkshire

Arevna Partners

 ...Device Manufacturer who are looking for a consultant to provide technical writing support for conversion of existing Technical Files to an MDR compliant format and providing consultative advice on gap analysis. Role includes: ~Interpret & assess domestic and global regulatory... 
North Yorkshire
more than 2 months ago

Programme Coordinator - MDR LAB (9 month FTC)

Mishcon de Reya

 ...being undertaken. In addition to a wide portfolio of transformational projects, the strategy team are also responsible for running MDR LAB – our LegalTech incubator programme. As the first dedicated legal incubator in the UK, the programme has played a key role in accelerating... 
London
27 days ago

Future Proofing your Business with MDR - The Next Steps

NetEDI Ltd

We’d like to pass on a massive thank you to the 100s of you who signed up to our recent webinar, Future Proofing your Business with MDR – Why it matters. This webinar presented us with an excellent opportunity to address many of your comments and queries regarding your relationship... 
Leyland, Lancashire
more than 2 months ago

Webinar: ‘Future proofing your business with Medical Device Regulations (MDR) - Why it matters’

NetEDI Ltd

 ...changes happening within the NHS Supply Chain right now in our free webinar, ‘Future proofing your business with Medical Device Regulations (MDR) – Why it matters’. Who will be hosting? Steve Moore, NetEDI’s newly-appointed Head of Healthcare Industry Development, will be... 
Preston, Lancashire
more than 2 months ago

Quality Engineer

PSG Global Solutions

 .../Medical Devices industry in , . Supports document changes, review of technical documents, plans and reports as it relates to EU MDR and other regulatory/standards compliance. Collaborates with operations, manufacturing, engineering, and regulatory functions to ensure... 
USA
11 days ago
new

Senior Regulatory Engineer

Honeywell

 ...chosen sites becoming ISO 13485 compliant Knowledge of the EUMDR Unique Device Identification requirement Identify and support new MDR and PPE regulatory standard changes to products Drive required MDR general support for registration, certification, audit of cGMP of... 
Bracknell, Berkshire
6 days ago

Financial Accountant

Mishcon de Reya LLP

 ...responsibility for managing asset leasing schedule; • Preparation of cost and overhead budgets; • Full responsibility for the accounting of MDR Discover LLP, including reconciliations, monthly management accounts, quarterly VAT returns and annual accounts preparation; • Review... 
London
17 days ago

Medical Writer

ConvaTec

 ...Performance (SSCP) documentation for inclusion in device technical documentation, in accordance with the Medical Device Regulation (EU MDR (EU) (2017/745) and internal Standard Operating Procedures (SOPs) Help with protocols / surveys for PMCFs and help prepare study reports... 
Deeside, Flintshire
10 days ago
new

Operations Quality Manager

CMR Surgical Ltd,

 ...achieving and maintaining compliance of business processes (e.g. QMS to ISO 13485) and the regulatory status of products (e.g. CE/MDD/MDR and US FDA 510(k) or PMA etc.) Acting as delegated responsibility for Management Representative role in the absence of the COO Providing... 
Cambridge, Cambridgeshire
2 days ago
new

SOC Analyst

£40k per annum

Lawrence Harvey.

 ...Benefits Location: Reading I'm currently working with one of the fastest growing Cyber Security Managed Detection & Response (MDR) firms in the UK who are continuing their expansion and looking to bring in a SOC Analyst. The successful candidate will be working... 
Reading, Berkshire
3 days ago
new

Business Analyst

£55k - £65k per annum

Anson McCade

 ...Business Analyst (HealthTech, MediTech, Start-up, Regulatory, MDD, MDR) Quick Summary: Become a part of our revolutionary HealthTech Start-up building a product that is positively impacting lives globally - currently we have circa 10 million users! We are dedicated... 
London
2 days ago

Biosafety Manager

Corin

 ...experience of working with the ISO 10993 series. ~ Also have experience with the following standards; 21 CFR 820.75, ISO 13485, MDD, MDR, ASTM, ISO 19227, ISO 14971. A degree in a scientific discipline required e.g. Biology, Biochemistry or Biomedical engineering.... 
Cirencester, Gloucestershire
12 days ago

Regulatory Affairs Associate

Carrot Pharma Recruitment

 ...following skills and experience; Good regulatory experience within medical devices (ideally up to class III) Good knowledge of MDD/MDR (desirable) Good knowledge of ISO 134585 Ideally experienced in managing registrations in EMEA, LATAM & APAC (desirable not... 
England
9 days ago
new

Senior Sales Business

Armored Pangolin

 ...may accept relevant experience. IT related degrees a plus. MBA a plus Familiarity with US and UK sales regulations is preferable. Experience selling to MSP providers, SMB IT companies, Financial sector is a plus Experience selling SOC/MDR/MSSP solutions is a plus... 
London
18 days ago
new

SECURITY CONSULTANT

F-Secure

 ...to join our global team to help successfully deliver our Managed Detection and Response service. Our Managed Detection and Response (MDR) business provides a world leading managed service that detects and responds to cyber-attacks on behalf of our clients using a strong... 
London
2 days ago

Regulatory Manager

Real Staffing

 ...Ideally educated to degree level or equivalent work experience * Understanding of ISO 13485, 14971, EN980, ISO11135, MDD 93/42/EEC AND MDR 2017/45 To find out more about Real please visit Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment... 
Cardiff
28 days ago
new

Biocompatibility Specialist

CK Group

 ...and the support Product, Biocompatibility, Manufacturing Processes, Sterilization, Packaging and/or Cleaning Validation information for MDR transformation. Understand and identify possible gaps for ISO 10993-1 and supporting ISO 10993 testing where needed. Develop... 
Switzerland
21 days ago

Expert Regulatory Specialist

Philips

 ...the opportunity to Provide expert regulatory support for Image Guided Therapy and execute PMAs for implantable devices in the US, EU MDR transition. Be recognized as a Regulatory Expert in US, EU, and other regional Regulatory filings. Be considered a vital... 
Plymouth, Devon
10 days ago
new

Associate - Commercial Litigation (NQ)

Mishcon de Reya LLP

 ...Group and membership of LegalLink gives us a reach far outside our London and New York homes. Technology underpins everything we do. MDR Discover, our in-house team of eDiscovery experts, reduces the cost and complexity of large-scale litigation. We invite legal start-ups... 
London
1 day ago